Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3390/separations10020108 http://hdl.handle.net/11449/248418 |
Resumo: | The synthesis of an organofunctionalized mesoporous silica was accomplished by a two-step process involving (1) the co-condensation of a silylant agent at the surface of silica, followed by (2) the immobilization of Purpald (ligand) at the organic termination of the silytant agent. The characterization of the organofunctionalized material indicated the presence of NH2 groups, and the immobilization of the ligand was confirmed by 29Si- and 13C-nuclear magnetic resonance. The material’s surface area was determined as 370 m2 g−1. Batch adsorption experiments enabled the determination of optimum pH conditions for the adsorption of Cu(II) and Cd(II). Under optimal pH, the pseudo-second-order kinetic model and Langmuir model provided the best correlations to describe the materials adsorption behavior, suggesting a chemisorption mechanism. When tested in continuous-flow preconcentration experiments, the flow rate and eluent concentration demonstrated to affect the removal of Cu(II) and Cd(II), while the buffer concentration had an effect only over the adsorption of Cu(II). Under optimized preconcentration conditions, it was possible both to determine the concentrations of Cu(II) and Cd(II) in samples such as mineral water, ground water, tap water and river water. Ions commonly found in drinking and natural waters (Na+, K+, Ca2+, Mg2+, Fe3+, Ba2+, Cl−, SO42−, HCO3−, and H2PO4−) did not affect the preconcentration of any of the studied analytes. Reutilization experiments indicated that the adsorbent material can withstand at least 40 adsorption/desorption preconcentration cycles with no efficiency loss. |
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Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extractionadsorptionpreconcentrationsolid-phase extractiontoxic metalsThe synthesis of an organofunctionalized mesoporous silica was accomplished by a two-step process involving (1) the co-condensation of a silylant agent at the surface of silica, followed by (2) the immobilization of Purpald (ligand) at the organic termination of the silytant agent. The characterization of the organofunctionalized material indicated the presence of NH2 groups, and the immobilization of the ligand was confirmed by 29Si- and 13C-nuclear magnetic resonance. The material’s surface area was determined as 370 m2 g−1. Batch adsorption experiments enabled the determination of optimum pH conditions for the adsorption of Cu(II) and Cd(II). Under optimal pH, the pseudo-second-order kinetic model and Langmuir model provided the best correlations to describe the materials adsorption behavior, suggesting a chemisorption mechanism. When tested in continuous-flow preconcentration experiments, the flow rate and eluent concentration demonstrated to affect the removal of Cu(II) and Cd(II), while the buffer concentration had an effect only over the adsorption of Cu(II). Under optimized preconcentration conditions, it was possible both to determine the concentrations of Cu(II) and Cd(II) in samples such as mineral water, ground water, tap water and river water. Ions commonly found in drinking and natural waters (Na+, K+, Ca2+, Mg2+, Fe3+, Ba2+, Cl−, SO42−, HCO3−, and H2PO4−) did not affect the preconcentration of any of the studied analytes. Reutilization experiments indicated that the adsorbent material can withstand at least 40 adsorption/desorption preconcentration cycles with no efficiency loss.Universidade Estadual PaulistaFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Faculty of Science and Technology University of Grande Dourados, Rodovia Dourados-Itahum, km 12, MSInterdisciplinary Laboratory of Nanostructures and Semiconductors (LINSE-IQ-UNESP), Rua Francisco Degni, 55, SPChemistry and Biochemistry Department Institute of Biosciences of Botucatu-UNESP, C.P. 510, SPInstituto de Física de São Carlos (IFSC) Universidade de São Paulo (USP), SPInterdisciplinary Laboratory of Nanostructures and Semiconductors (LINSE-IQ-UNESP), Rua Francisco Degni, 55, SPChemistry and Biochemistry Department Institute of Biosciences of Botucatu-UNESP, C.P. 510, SPFAPESP: 2015/04791-8FAPESP: 2018/18787-0CNPq: 312361/2021-1University of Grande DouradosUniversidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Wondracek, Marcos Henrique PereiraJorgetto, Alexandre de Oliveira [UNESP]da Silva, Adrielli Cristina Peres [UNESP]Schneider, José FabiánPedrosa, Valber de Albuquerque [UNESP]Saeki, Margarida Juri [UNESP]de Castro, Gustavo Rocha [UNESP]2023-07-29T13:43:28Z2023-07-29T13:43:28Z2023-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/separations10020108Separations, v. 10, n. 2, 2023.2297-8739http://hdl.handle.net/11449/24841810.3390/separations100201082-s2.0-85148876835Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengSeparationsinfo:eu-repo/semantics/openAccess2023-07-29T13:43:28Zoai:repositorio.unesp.br:11449/248418Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:57:02.309291Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction |
title |
Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction |
spellingShingle |
Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction Wondracek, Marcos Henrique Pereira adsorption preconcentration solid-phase extraction toxic metals |
title_short |
Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction |
title_full |
Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction |
title_fullStr |
Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction |
title_full_unstemmed |
Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction |
title_sort |
Synthesis and Characterization of Mesoporous Silica Modified with Purpald and Its Application in the Preconcentration of Cu2+ and Cd2+ from Aqueous Samples through Solid-Phase Extraction |
author |
Wondracek, Marcos Henrique Pereira |
author_facet |
Wondracek, Marcos Henrique Pereira Jorgetto, Alexandre de Oliveira [UNESP] da Silva, Adrielli Cristina Peres [UNESP] Schneider, José Fabián Pedrosa, Valber de Albuquerque [UNESP] Saeki, Margarida Juri [UNESP] de Castro, Gustavo Rocha [UNESP] |
author_role |
author |
author2 |
Jorgetto, Alexandre de Oliveira [UNESP] da Silva, Adrielli Cristina Peres [UNESP] Schneider, José Fabián Pedrosa, Valber de Albuquerque [UNESP] Saeki, Margarida Juri [UNESP] de Castro, Gustavo Rocha [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
University of Grande Dourados Universidade Estadual Paulista (UNESP) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Wondracek, Marcos Henrique Pereira Jorgetto, Alexandre de Oliveira [UNESP] da Silva, Adrielli Cristina Peres [UNESP] Schneider, José Fabián Pedrosa, Valber de Albuquerque [UNESP] Saeki, Margarida Juri [UNESP] de Castro, Gustavo Rocha [UNESP] |
dc.subject.por.fl_str_mv |
adsorption preconcentration solid-phase extraction toxic metals |
topic |
adsorption preconcentration solid-phase extraction toxic metals |
description |
The synthesis of an organofunctionalized mesoporous silica was accomplished by a two-step process involving (1) the co-condensation of a silylant agent at the surface of silica, followed by (2) the immobilization of Purpald (ligand) at the organic termination of the silytant agent. The characterization of the organofunctionalized material indicated the presence of NH2 groups, and the immobilization of the ligand was confirmed by 29Si- and 13C-nuclear magnetic resonance. The material’s surface area was determined as 370 m2 g−1. Batch adsorption experiments enabled the determination of optimum pH conditions for the adsorption of Cu(II) and Cd(II). Under optimal pH, the pseudo-second-order kinetic model and Langmuir model provided the best correlations to describe the materials adsorption behavior, suggesting a chemisorption mechanism. When tested in continuous-flow preconcentration experiments, the flow rate and eluent concentration demonstrated to affect the removal of Cu(II) and Cd(II), while the buffer concentration had an effect only over the adsorption of Cu(II). Under optimized preconcentration conditions, it was possible both to determine the concentrations of Cu(II) and Cd(II) in samples such as mineral water, ground water, tap water and river water. Ions commonly found in drinking and natural waters (Na+, K+, Ca2+, Mg2+, Fe3+, Ba2+, Cl−, SO42−, HCO3−, and H2PO4−) did not affect the preconcentration of any of the studied analytes. Reutilization experiments indicated that the adsorbent material can withstand at least 40 adsorption/desorption preconcentration cycles with no efficiency loss. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T13:43:28Z 2023-07-29T13:43:28Z 2023-02-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3390/separations10020108 Separations, v. 10, n. 2, 2023. 2297-8739 http://hdl.handle.net/11449/248418 10.3390/separations10020108 2-s2.0-85148876835 |
url |
http://dx.doi.org/10.3390/separations10020108 http://hdl.handle.net/11449/248418 |
identifier_str_mv |
Separations, v. 10, n. 2, 2023. 2297-8739 10.3390/separations10020108 2-s2.0-85148876835 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Separations |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
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1808129265832558592 |